Newbie
Hi everyone my name is Marcela I am 44 years old and was diagnosed last year October the 1st with Her2 positive metastatic BC. The cancer has spread to my liver and bones (spine, pelvis and some on my ribs). This was my initial diagnosis. So as you all know just getting a diagnosis of BC is traumatising enough but to be told it has spread and that there is no cure was devastating for me and my family. I felt like I was dreaming when the doctor was talking to my husband and I in her surgery that day, because there is no-one in my family with BC. My words to the doctor were- just cut them off! as I didn't know a single thing about BC let alone Her2+ or that it was too late because of the spread. I have always been healthy and into exercise and since receiving my diagnosis I have devoted myself to an anti cancer diet and way of life. I try hard to stay as healthy as possible to live as long as I can with this, to hopefully miraculously go into remission.... or stay around long enough for new treatments or hopefully a cure for us all!
When I was waiting to start treatment within that week in October last year the cancer fractured my spine. All I was doing was getting up from being seated on the lounge! The pain was excruciating and I have had children naturally so thats saying something! They had to give me so much pain medicine just to have me put my legs down to have me go through the CT machine. Every time they moved me the pain was through the roof, even with all the meds. They warned my husband that I may not walk again.....they eventually got me through the CT machine and they recommended to my husband that I have radiation on my spine. I was in no condition to make decisions because of the amount of meds to control the pain. I had the radiation and recovered in hospital for 3 weeks. In those 3 weeks I walked! And since then I have come a long way. They give me a bone strengthening injection with my treatment to prevent further fractures. I had chemo for 5 months along with Herceptin and Perjeta. I am currently having a break from chemo but I am on Herceptin and Perjeta as long as they continue to work.
I would have to stay one of the hardest things through this is the mental turmoil. As you all know we have our good days and bad days. I guess being faced with your mortality is something that people who have cancer or have had cancer know all about to well. I previously had my own business and worked very hard. Since being diagnosed I gave that all away and focus solely on living! I focus on my family and my health. I guess my cancer diagnosis really gave me a wake up call and made me realise what is important for me. Take you for reading my story ladies, I wish you all the best of health. See you all here soon! :)
I posted his on the main page. But I thought I would post this here to see if I could find ladies here in a similar situation.
